Canonical Allele Identifier: CA727854033

Gene: TAOK1

Linked Data

• dbSNP Id: rs1208131620
• gnomAD v3: 17-29477483-A-ATT
• gnomAD v4: 17-29477483-A-ATT
• MyVariant Identifiers: chr17:g.27804501_27804502insTT (hg19) ; chr17:g.29477483_29477484insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29477486_29477487dup , CM000679.2:g.29477486_29477487dup	GRCh38
NC_000017.10:g.27804504_27804505dup , CM000679.1:g.27804504_27804505dup	GRCh37
NC_000017.9:g.24828630_24828631dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261716.8:c.307-175_307-174dup MANE Select	ENSP00000261716.3:n.307-175_307-174dup
ENST00000261716.7:c.307-175_307-174dup	ENSP00000261716.3:n.307-175_307-174dup
ENST00000536202.1:c.307-175_307-174dup	ENSP00000438819.1:n.307-175_307-174dup
NM_020791.2:c.307-175_307-174dup	NP_065842.1:n.307-175_307-174dup
NM_025142.1:c.307-175_307-174dup	NP_079418.1:n.307-175_307-174dup
XM_011525060.1:c.307-175_307-174dup	XP_011523362.1:n.307-175_307-174dup
XM_011525060.2:c.307-175_307-174dup	XP_011523362.1:n.307-175_307-174dup
NM_020791.4:c.307-175_307-174dup MANE Select	NP_065842.1:n.307-175_307-174dup